SLC26A6 Gene Hyperoxaluria SLC26A6 Related NGS Genetic DNA Test
Introduction
The SLC26A6 Gene Hyperoxaluria NGS Genetic Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with hyperoxaluria, a metabolic disorder that can lead to kidney stones and renal failure. Understanding your genetic predisposition is crucial for effective management and treatment of this condition.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to analyze the SLC26A6 gene, which plays a significant role in oxalate transport and metabolism in the body. By detecting mutations in this gene, healthcare providers can assess the risk of hyperoxaluria and its complications.
Who Should Consider This Test
Individuals with a family history of hyperoxaluria or those experiencing symptoms such as recurrent kidney stones, renal insufficiency, or metabolic disorders should consider this test. Risk factors include:
- Family history of metabolic disorders
- Personal history of kidney stones
- Symptoms of renal dysfunction
Benefits of Taking the Test
Taking the SLC26A6 Gene Hyperoxaluria NGS Genetic Test offers numerous benefits:
- Early identification of genetic predispositions
- Informed decision-making for treatment options
- Guidance for family planning and genetic counseling
- Personalized management strategies for metabolic disorders
Understanding Your Results
Results from the SLC26A6 Gene Hyperoxaluria NGS Genetic Test will indicate whether any mutations are present. A genetic counselor will assist in interpreting the results and discussing their implications for your health and family.
Test Details
| Test Name | Price (NGN) |
|---|---|
| SLC26A6 Gene Hyperoxaluria SLC26A6 Related NGS Genetic DNA Test | Discount Price: 400000 NGN Regular Price: 560000 NGN |
Booking the Test
To book the SLC26A6 Gene Hyperoxaluria NGS Genetic Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and answering any questions you may have.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One Drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by hyperoxaluria.
For comprehensive insights into your genetic health concerning metabolic disorders, consider the SLC26A6 Gene Hyperoxaluria NGS Genetic Test today!
